ENST00000463045.3:c.223C>A
|
ENSP00000481376.2:p.His75Asn
|
|
ENST00000491274.6:c.352C>A
|
ENSP00000480482.2:p.His118Asn
|
|
ENST00000375499.8:c.394C>A
MANE Select
|
ENSP00000364649.3:p.His132Asn
|
|
ENST00000375499.7:c.394C>A
|
ENSP00000364649.3:p.His132Asn
|
|
ENST00000463045.2:c.223C>A
|
ENSP00000481376.1:p.His75Asn
|
|
ENST00000475506.1:n.311C>A
|
|
|
ENST00000485515.5:n.357+25C>A
|
|
|
ENST00000491274.5:c.352C>A
|
ENSP00000480482.1:p.His118Asn
|
|
NM_003000.2:c.394C>A , LRG_316t1:c.394C>A
|
NP_002991.2:p.His132Asn
|
|
NM_003000.3:c.394C>A
MANE Select
|
NP_002991.2:p.His132Asn
|
|